BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

230 related articles for article (PubMed ID: 29603867)

  • 1. Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications.
    Wolfe K; McQuillin A; Alesi V; Boudry Labis E; Cutajar P; Dallapiccola B; Dentici ML; Dieux-Coeslier A; Duban-Bedu B; Duelund Hjortshøj T; Goel H; Loddo S; Morrogh D; Mosca-Boidron AL; Novelli A; Olivier-Faivre L; Parker J; Parker MJ; Patch C; Pelling AL; Smol T; Tümer Z; Vanakker O; van Haeringen A; Vanlerberghe C; Strydom A; Skuse D; Bass N
    Am J Med Genet B Neuropsychiatr Genet; 2018 Jun; 177(4):397-405. PubMed ID: 29603867
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Recurrent deletions and duplications of chromosome 2q11.2 and 2q13 are associated with variable outcomes.
    Riley KN; Catalano LM; Bernat JA; Adams SD; Martin DM; Lalani SR; Patel A; Burnside RD; Innis JW; Rudd MK
    Am J Med Genet A; 2015 Nov; 167A(11):2664-73. PubMed ID: 26227573
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size.
    Shinawi M; Liu P; Kang SH; Shen J; Belmont JW; Scott DA; Probst FJ; Craigen WJ; Graham BH; Pursley A; Clark G; Lee J; Proud M; Stocco A; Rodriguez DL; Kozel BA; Sparagana S; Roeder ER; McGrew SG; Kurczynski TW; Allison LJ; Amato S; Savage S; Patel A; Stankiewicz P; Beaudet AL; Cheung SW; Lupski JR
    J Med Genet; 2010 May; 47(5):332-41. PubMed ID: 19914906
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A recurrent 1.71 Mb genomic imbalance at 2q13 increases the risk of developmental delay and dysmorphism.
    Yu HE; Hawash K; Picker J; Stoler J; Urion D; Wu BL; Shen Y
    Clin Genet; 2012 Mar; 81(3):257-64. PubMed ID: 21255006
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 17q12 Recurrent Deletions and Duplications: Description of a Case Series with Neuropsychiatric Phenotype.
    Milone R; Tancredi R; Cosenza A; Ferrari AR; Scalise R; Cioni G; Battini R
    Genes (Basel); 2021 Oct; 12(11):. PubMed ID: 34828266
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Small rare recurrent deletions and reciprocal duplications in 2q21.1, including brain-specific ARHGEF4 and GPR148.
    Dharmadhikari AV; Kang SH; Szafranski P; Person RE; Sampath S; Prakash SK; Bader PI; Phillips JA; Hannig V; Williams M; Vinson SS; Wilfong AA; Reimschisel TE; Craigen WJ; Patel A; Bi W; Lupski JR; Belmont J; Cheung SW; Stankiewicz P
    Hum Mol Genet; 2012 Aug; 21(15):3345-55. PubMed ID: 22543972
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders.
    Miller DT; Shen Y; Weiss LA; Korn J; Anselm I; Bridgemohan C; Cox GF; Dickinson H; Gentile J; Harris DJ; Hegde V; Hundley R; Khwaja O; Kothare S; Luedke C; Nasir R; Poduri A; Prasad K; Raffalli P; Reinhard A; Smith SE; Sobeih MM; Soul JS; Stoler J; Takeoka M; Tan WH; Thakuria J; Wolff R; Yusupov R; Gusella JF; Daly MJ; Wu BL
    J Med Genet; 2009 Apr; 46(4):242-8. PubMed ID: 18805830
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Adult neuropsychiatric expression and familial segregation of 2q13 duplications.
    Costain G; Lionel AC; Fu F; Stavropoulos DJ; Gazzellone MJ; Marshall CR; Scherer SW; Bassett AS
    Am J Med Genet B Neuropsychiatr Genet; 2014 Jun; 165B(4):337-44. PubMed ID: 24807792
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genotype-phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study.
    Chawner SJRA; Owen MJ; Holmans P; Raymond FL; Skuse D; Hall J; van den Bree MBM
    Lancet Psychiatry; 2019 Jun; 6(6):493-505. PubMed ID: 31056457
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders.
    Tropeano M; Ahn JW; Dobson RJ; Breen G; Rucker J; Dixit A; Pal DK; McGuffin P; Farmer A; White PS; Andrieux J; Vassos E; Ogilvie CM; Curran S; Collier DA
    PLoS One; 2013; 8(4):e61365. PubMed ID: 23637818
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Copy number variants analysis in a cohort of isolated and syndromic developmental delay/intellectual disability reveals novel genomic disorders, position effects and candidate disease genes.
    Di Gregorio E; Riberi E; Belligni EF; Biamino E; Spielmann M; Ala U; Calcia A; Bagnasco I; Carli D; Gai G; Giordano M; Guala A; Keller R; Mandrile G; Arduino C; Maffè A; Naretto VG; Sirchia F; Sorasio L; Ungari S; Zonta A; Zacchetti G; Talarico F; Pappi P; Cavalieri S; Giorgio E; Mancini C; Ferrero M; Brussino A; Savin E; Gandione M; Pelle A; Giachino DF; De Marchi M; Restagno G; Provero P; Cirillo Silengo M; Grosso E; Buxbaum JD; Pasini B; De Rubeis S; Brusco A; Ferrero GB
    Clin Genet; 2017 Oct; 92(4):415-422. PubMed ID: 28295210
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis.
    Williams NM; Zaharieva I; Martin A; Langley K; Mantripragada K; Fossdal R; Stefansson H; Stefansson K; Magnusson P; Gudmundsson OO; Gustafsson O; Holmans P; Owen MJ; O'Donovan M; Thapar A
    Lancet; 2010 Oct; 376(9750):1401-8. PubMed ID: 20888040
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders.
    Calle Sánchez X; Helenius D; Bybjerg-Grauholm J; Pedersen C; Hougaard DM; Børglum AD; Nordentoft M; Mors O; Mortensen PB; Geschwind DH; Montalbano S; Raznahan A; Thompson WK; Ingason A; Werge T
    JAMA Psychiatry; 2022 Jan; 79(1):59-69. PubMed ID: 34817560
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical and genetic findings in Hungarian pediatric patients carrying chromosome 16p copy number variants and a review of the literature.
    Lengyel A; Pinti É; Pikó H; Jávorszky E; David D; Tihanyi M; Gönczi É; Kiss E; Tóth Z; Tory K; Fekete G; Haltrich I
    Eur J Med Genet; 2020 Oct; 63(10):104027. PubMed ID: 32758661
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Psychiatric disorders in children with 16p11.2 deletion and duplication.
    Niarchou M; Chawner SJRA; Doherty JL; Maillard AM; Jacquemont S; Chung WK; Green-Snyder L; Bernier RA; Goin-Kochel RP; Hanson E; Linden DEJ; Linden SC; Raymond FL; Skuse D; Hall J; Owen MJ; Bree MBMVD
    Transl Psychiatry; 2019 Jan; 9(1):8. PubMed ID: 30664628
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis of 2q13 duplications: The crucial role of the family survey in genetic counseling on novel copy number variations.
    Bellil H; Molina-Gomes D; Quibel T; Roy S; Dard R; Vialard F; Herve B
    Eur J Med Genet; 2020 Aug; 63(8):103956. PubMed ID: 32439619
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition.
    Hippolyte L; Maillard AM; Rodriguez-Herreros B; Pain A; Martin-Brevet S; Ferrari C; Conus P; Macé A; Hadjikhani N; Metspalu A; Reigo A; Kolk A; Männik K; Barker M; Isidor B; Le Caignec C; Mignot C; Schneider L; Mottron L; Keren B; David A; Doco-Fenzy M; Gérard M; Bernier R; Goin-Kochel RP; Hanson E; Green Snyder L; ; Ramus F; Beckmann JS; Draganski B; Reymond A; Jacquemont S
    Biol Psychiatry; 2016 Jul; 80(2):129-139. PubMed ID: 26742926
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Int22h-1/int22h-2-mediated Xq28 rearrangements: intellectual disability associated with duplications and in utero male lethality with deletions.
    El-Hattab AW; Fang P; Jin W; Hughes JR; Gibson JB; Patel GS; Grange DK; Manwaring LP; Patel A; Stankiewicz P; Cheung SW
    J Med Genet; 2011 Dec; 48(12):840-50. PubMed ID: 21984752
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The interstitial duplication 15q11.2-q13 syndrome includes autism, mild facial anomalies and a characteristic EEG signature.
    Urraca N; Cleary J; Brewer V; Pivnick EK; McVicar K; Thibert RL; Schanen NC; Esmer C; Lamport D; Reiter LT
    Autism Res; 2013 Aug; 6(4):268-79. PubMed ID: 23495136
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Autism Spectrum Disorder, Developmental and Psychiatric Features in 16p11.2 Duplication.
    Green Snyder L; D'Angelo D; Chen Q; Bernier R; Goin-Kochel RP; Wallace AS; Gerdts J; Kanne S; Berry L; Blaskey L; Kuschner E; Roberts T; Sherr E; Martin CL; Ledbetter DH; Spiro JE; Chung WK; Hanson E;
    J Autism Dev Disord; 2016 Aug; 46(8):2734-2748. PubMed ID: 27207092
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.